Stryker Gmbh: Appliance, Fixation, Nail/blade/plate Combination, Multiple Component
Recall Summary Stryker GmbH is recalling the Hoffmann II Connecting Rod Micro (3 x 90mm, catalog number 50796090), a surgical fixation device, because the carbon rods may crack after being cleaned and sterilized. The product was distributed worldwide, including throughout the United States and multiple other countries. This is a Class II recall, indicating a potential serious health risk.
- Recalling firm
- Stryker GmbH
- Product
- Stryker Hoffmann II Connecting Rod Micro 3 x 90mm. Catalog Number: 50796090.
- Reason
- Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.
- Classification
- Class II
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-07-01
- Status
- Open, Classified
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- Worldwide - US Nationwide distribution including in the states of AL, AZ, CA, CO, FL, GA, ID, IL, KS, LA, MA, MD, MI, MN, MO, MT, NC, NE, NH, NJ, NM, NY, OH, PA, RI, SC, TN, TX, VA, WI, WV and the countries of Australia, Austria, Belgium, Canada, Chile, Denmark, France, Germany, Greece, Ireland,...
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/0e812ead-053e-4a80-94eb-9874d80c79b8